Abstract

The mechanics of complex soft matter often cannot be understood in the classical physical frame of flexible polymers or rigid rods. The underlying constituents are semiflexible polymers, whose finite bending stiffness (κκ) leads to non-trivial mechanical responses. A natural model for such polymers is the protein actin. Experimental studies of actin networks, however, are limited since the persistence length (lp∝κl_{\text{p}} \propto κ) cannot be tuned. Here, we experimentally characterize this parameter for the first time in entangled networks formed by synthetically produced, structurally tunable DNA nanotubes. This material enabled the validation of characteristics inherent to semiflexible polymers and networks thereof, i.e., persistence length, inextensibility, reptation and mesh size scaling. While the scaling of the elastic plateau modulus with concentration G0∝c7/5G_0 \propto c^{7/5} is consistent with previous measurements and established theories, the emerging persistence length scaling G0∝lpG_0 \propto l_{\text{p}} opposes predominant theoretical predictions.

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